AnnotSV

Compiles functionally and clinically relevant information to interpret SV pathogenicity quickly.

What it does

Integrates databases like DGV to compute allelic frequencies for structural variations, rapidly filtering out common benign macro-events.

How to use

See https://lbgi.fr/AnnotSV/ for documentation and access.

STRC usage

Not directly applicable to E1659A via API. Requires local installation or web interface. See documentation for manual usage.

Connections

• STRC Variant c.4976A>C — Misha [see-also]
• STRC Gene [about]
• [part-of] Tools index